MGI MP annotations for MGI:102551: Ccnf

Gray arrows indicate "is_a"



Compare annotations to MP categories for MGI:102551.

• Entry indicates phenotypic allele for this gene.
• Colored entries indicate MP annotation.

ID	Term	Ccnftm1.1Sje
MP:0005385	cardiovascular system phenotype	Ccnftm1.1Sje
MP:0005384	cellular phenotype	Ccnftm1.1Sje
MP:0005380	embryogenesis phenotype	Ccnftm1.1Sje
MP:0005378	growth/size phenotype	Ccnftm1.1Sje
MP:0005371	limbs/digits/tail phenotype	Ccnftm1.1Sje
MP:0010768	mortality/aging	Ccnftm1.1Sje
MP:0003631	nervous system phenotype	Ccnftm1.1Sje

Full set of annotations for MGI:102551

ID	Term	Allele	Alleles	Background	Color Key
MP:0001726	abnormal allantois morphology	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003077	abnormal cell cycle	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003232	abnormal forebrain development	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0006108	abnormal hindbrain development	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0005650	abnormal limb bud morphology	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003864	abnormal midbrain development	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003720	abnormal neural tube closure	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001712	abnormal placenta development	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0005221	abnormal rostral-caudal axis patterning	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001718	abnormal visceral yolk sac morphology	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0004076	abnormal vitelline vascular remodeling	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003229	abnormal vitelline vasculature morphology	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001719	absent vitelline blood vessels	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0011098	complete embryonic lethality during organogenesis	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0000352	decreased cell proliferation	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001698	decreased embryo size	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001889	delayed brain development	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001723	disorganized yolk sac vascular plexus	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0009657	failure of chorioallantoic fusion	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001701	incomplete embryo turning	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0003400	kinked neural tube	Ccnftm1.1Sje	Ccnftm1.1Sje/Ccnftm1.1Sje	involves: 129S7/SvEvBrd * C57BL/6	color key